Excedrin - 0067-2030-91 - (Acetaminophen, Aspirin (NSAID), and Caffeine)

Alphabetical Index


Drug Information of Excedrin

Product NDC: 0067-2030
Proprietary Name: Excedrin
Non Proprietary Name: Acetaminophen, Aspirin (NSAID), and Caffeine
Active Ingredient(s): 250; 250; 65    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Aspirin (NSAID), and Caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Excedrin

Product NDC: 0067-2030
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20060927

Package Information of Excedrin

Package NDC: 0067-2030-91
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0067-2030-91) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Excedrin

NDC Code 0067-2030-91
Proprietary Name Excedrin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0067-2030-91) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 0067-2030
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Aspirin (NSAID), and Caffeine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060927
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Novartis Consumer Health, Inc.
Substance Name ACETAMINOPHEN; ASPIRIN; CAFFEINE
Strength Number 250; 250; 65
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Excedrin


General Information